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Monodisperse Thermoresponsive Microgels with Tunable Volume-Phase Transition Kinetics.
- Published in:
- Advanced Functional Materials, 2007, v. 17, n. 17, p. 3499, doi. 10.1002/adfm.200700379
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- Publication type:
- Article
On a finite element CFD algorithm for compressible, viscous and turbulent aerodynamic flows.
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- International Journal for Numerical Methods in Fluids, 1987, v. 7, n. 11, p. 1235, doi. 10.1002/fld.1650071107
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- Publication type:
- Article
A taylor weak-statement algorithm for hyperbolic conservation laws.
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- International Journal for Numerical Methods in Fluids, 1987, v. 7, n. 5, p. 489, doi. 10.1002/fld.1650070505
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- Publication type:
- Article
Body motion detection and correction in cardiac PET: Phantom and human studies.
- Published in:
- Medical Physics, 2019, v. 46, n. 11, p. 4898, doi. 10.1002/mp.13815
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- Publication type:
- Article
In-vitro and in-vivo antibacterial activity of CFC-222, a new fluoroquinolone.
- Published in:
- 1998
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- Publication type:
- journal article
Skin cell targeting with self-assembled ligand addressed nanoemulsion droplets.
- Published in:
- International Journal of Cosmetic Science, 2013, v. 35, n. 3, p. 310, doi. 10.1111/ics.12044
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- Publication type:
- Article
The stabilization of L-ascorbic acid in aqueous solution and water-in-oil-in-water double emulsion by controlling pH and electrolyte concentration.
- Published in:
- 2004
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- Publication type:
- Abstract
Determination of Panthenol, Cholecalciferol and Tocopherol in Cosmetic Products by Gas Chromatography-Mass Spectrometry in SIM Mode.
- Published in:
- International Journal of Cosmetic Science, 1999, v. 21, n. 1, p. 41, doi. 10.1046/j.1467-2494.1999.181685.x
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- Publication type:
- Article
Comparison of HPV DNA vaccines employing intracellular targeting strategies.
- Published in:
- Gene Therapy, 2004, v. 11, n. 12, p. 1011, doi. 10.1038/sj.gt.3302252
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- Publication type:
- Article
Ground-state correlations and finite temperature properties of the transverse Ising model.
- Published in:
- European Physical Journal B: Condensed Matter, 2005, v. 43, n. 3, p. 373, doi. 10.1140/epjb/e2005-00066-x
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- Publication type:
- Article
Increased immunoreactivity for TRPM8 in cutaneous squamous cell carcinoma.
- Published in:
- Journal of Cutaneous Pathology, 2018, v. 45, n. 12, p. 970, doi. 10.1111/cup.13358
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- Publication type:
- Article
A novel ACAD8 mutation in asymptomatic patients with isobutyryl- CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 2, p. 196, doi. 10.1111/cge.12350
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- Publication type:
- Article
Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 1, p. 90, doi. 10.1111/cge.12340
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- Publication type:
- Article
Frequency of DMPK mutation carriers in Korean women of childbearing age.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 4, p. 398, doi. 10.1111/cge.12310
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- Publication type:
- Article
Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 5, p. 441, doi. 10.1111/cge.12195
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- Publication type:
- Article
Identification of 11 novel mutations in 49 Korean patients with mucopolysaccharidosis type II.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 2, p. 185, doi. 10.1111/j.1399-0004.2011.01641.x
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- Publication type:
- Article
Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 4, p. 378, doi. 10.1111/j.1399-0004.2010.01483.x
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- Publication type:
- Article
Clinical and genetic analysis of Korean patients with Marfan syndrome: possible ethnic differences in clinical manifestation.
- Published in:
- Clinical Genetics, 2010, v. 77, n. 2, p. 177, doi. 10.1111/j.1399-0004.2009.01287.x
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- Publication type:
- Article
Clinical and genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome.
- Published in:
- 2009
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- Publication type:
- Letter
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.
- Published in:
- 2006
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- Publication type:
- Letter
Genetic basis of Prader–Willi syndrome in Korea: less uniparental disomy than has been recognized?
- Published in:
- 2004
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- Publication type:
- Letter
Mutation spectrum of the glucose-6-phosphatase gene and its implication in molecular diagnosis of Korean patients with glycogen storage disease type Ia.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 6, p. 487, doi. 10.1111/j.1399-0004.2004.00260.x
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- Publication type:
- Article
Paradoxical embolism as a cause of silent brain infarctions in healthy subjects: the ICONS study ( Identification of the Cause of Silent Cerebral Infarction in Healthy Subjects).
- Published in:
- European Journal of Neurology, 2013, v. 20, n. 2, p. 353, doi. 10.1111/j.1468-1331.2012.03864.x
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- Publication type:
- Article
Dystonic head tremor associated with a parietal lesion.
- Published in:
- 2007
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- Publication type:
- Letter
Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta.
- Published in:
- Journal of Dental Research, 2022, v. 101, n. 1, p. 37, doi. 10.1177/00220345211015119
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- Publication type:
- Article
Alteration of Exon Definition Causes Amelogenesis Imperfecta.
- Published in:
- 2020
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- Publication type:
- journal article
WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis.
- Published in:
- 2019
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- Publication type:
- journal article
Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations.
- Published in:
- 2018
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- Publication type:
- journal article
Efficacy of rhBMP-2/Hydroxyapatite on Sinus Floor Augmentation: A Multicenter, Randomized Controlled Clinical Trial.
- Published in:
- 2015
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- Publication type:
- journal article
Efficacy of rhBMP-2/Hydroxyapatite on Sinus Floor Augmentation.
- Published in:
- Journal of Dental Research, 2015, v. 94, p. 158S, doi. 10.1177/0022034515594573
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- Publication type:
- Article
Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.
- Published in:
- 2015
- By:
- Publication type:
- Journal Article
COUP-TFII Stimulates Dentin Sialophosphoprotein Expression and Mineralization in Odontoblasts.
- Published in:
- 2015
- By:
- Publication type:
- Journal Article
Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.
- Published in:
- Journal of Dental Research, 2015, v. 94, n. 8, p. 1063, doi. 10.1177/0022034515590569
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- Publication type:
- Article
COUP-TFII Stimulates Dentin Sialophosphoprotein Expression and Mineralization in Odontoblasts.
- Published in:
- Journal of Dental Research, 2015, v. 94, n. 8, p. 1135, doi. 10.1177/0022034515585125
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- Publication type:
- Article
ENAM mutations with incomplete penetrance.
- Published in:
- 2014
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- Publication type:
- journal article
ENAM Mutations with Incomplete Penetrance.
- Published in:
- Journal of Dental Research, 2014, v. 93, n. 10, p. 988, doi. 10.1177/0022034514548222
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- Publication type:
- Article
Alteration of Conserved Alternative Splicing in AMELX Causes Enamel Defects.
- Published in:
- Journal of Dental Research, 2014, v. 93, n. 10, p. 980, doi. 10.1177/0022034514547272
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- Publication type:
- Article
Exonal Deletion of SLC24A4 Causes Hypomaturation Amelogenesis Imperfecta.
- Published in:
- Journal of Dental Research, 2014, v. 93, n. 4, p. 366, doi. 10.1177/0022034514523786
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- Publication type:
- Article
Association between interleukin-4 gene polymorphisms and intracerebral haemorrhage in Korean population.
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- International Journal of Immunogenetics, 2011, v. 38, n. 4, p. 321, doi. 10.1111/j.1744-313X.2011.01010.x
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- Publication type:
- Article
Landscape of Elderly Suicide in South Korea: Its Trend According to Age, Gender, and Educational Attainment.
- Published in:
- Omega: Journal of Death & Dying, 2020, v. 82, n. 2, p. 214, doi. 10.1177/0030222818807845
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- Publication type:
- Article
Liquid crystal added electrorheological fluid.
- Published in:
- Journal of Materials Science Letters, 2003, v. 22, n. 11, p. 807, doi. 10.1023/A:1023956007971
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- Publication type:
- Article
Electrical properties of the Pt/Sr<sub>0.85</sub>Bi<sub>2.4</sub>Ta<sub>2</sub>O<sub>9</sub>/TiO<sub>2</sub>/Si structure with variation of the Sr<sub>0.85</sub>Bi<sub>2.4</sub>Ta<sub>2</sub>O<sub>9</sub> film thickness.
- Published in:
- Journal of Materials Science Letters, 2003, v. 22, n. 7, p. 535, doi. 10.1023/A:1022994521453
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- Publication type:
- Article
Topiramate stimulates glucose transport through AMP-activated protein kinase-mediated pathway in L6 skeletal muscle cells.
- Published in:
- Pharmacogenomics Journal, 2006, v. 6, n. 5, p. 327, doi. 10.1038/sj.tpj.6500366
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- Publication type:
- Article
Diel activity patterns of the fish community in a temperate stream.
- Published in:
- Journal of Fish Biology, 2013, v. 82, n. 5, p. 1700, doi. 10.1111/jfb.12071
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- Publication type:
- Article
Combined effects of chemical and visual information in eliciting antipredator behaviour in juvenile Atlantic salmon Salmo salar.
- Published in:
- Journal of Fish Biology, 2009, v. 74, n. 6, p. 1280, doi. 10.1111/j.1095-8649.2009.02199.x
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- Publication type:
- Article
P01-188 - Regional brain perfusion differences associated with norepinephrine transporter gene polymorphisms in ADHD
- Published in:
- 2010
- By:
- Publication type:
- Abstract
TEM and XRD determination of crystallite size and lattice strain as a function of illite crystallinity in pelitic rocks.
- Published in:
- Journal of Metamorphic Geology, 1997, v. 15, n. 2, p. 267, doi. 10.1111/j.1525-1314.1997.00016.x
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- Publication type:
- Article
Two novel mutations in the EPM2A gene in a Korean patient with Lafora's progressive myoclonus epilepsy.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 1, p. 51, doi. 10.1007/s100380300006
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- Publication type:
- Article
A novel missense mutation (I344K) in the SPG4 gene in a Korean family with autosomal-dominant hereditary spastic paraplegia.
- Published in:
- Journal of Human Genetics, 2002, v. 47, n. 9, p. 473, doi. 10.1007/s100380200068
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- Publication type:
- Article
Identification of lamin A/C (LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
- Published in:
- Journal of Human Genetics, 2002, v. 47, n. 5, p. 225, doi. 10.1007/s100380200029
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- Publication type:
- Article